The lack of either IRF9, or STAT2, has surprisingly little effect on human natural killer cell development and function

Analysis of genetically defined immunodeficient patients allows study of the effect of the absence of specific proteins on human immune function in real-world conditions. Here we have addressed the importance of type I interferon signalling for human NK cell development by studying the phenotype and...

Descripción completa

Detalles Bibliográficos
Autores: Calvo-Apalategi, Ane, Nevado, Marta López, Bravo-Gallego, Luz Yadira, González-Granado, Luis Ignacio, Allende, Luis M, Pena, Rebeca Rodríguez, López-Granados, Eduardo, Reyburn, H. T.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/359244
Acceso en línea:http://hdl.handle.net/10261/359244
https://api.elsevier.com/content/abstract/scopus_id/85189068085
Access Level:acceso abierto
Palabra clave:NK cell
Cytokines
Immune deficiencies
Descripción
Sumario:Analysis of genetically defined immunodeficient patients allows study of the effect of the absence of specific proteins on human immune function in real-world conditions. Here we have addressed the importance of type I interferon signalling for human NK cell development by studying the phenotype and function of circulating NK cells isolated from patients suffering primary immunodeficiency disease due to mutation of either the human interferon regulatory factor 9 (IRF9) or the signal transducer and activator of transcription 2 (STAT2) genes. IRF9, together with phosphorylated STAT1 and STAT2, form a heterotrimer called interferon stimulated gene factor 3 (ISGF3) which promotes the expression of hundreds of IFN-stimulated genes that mediate antiviral function triggered by exposure to type I interferons. IRF9- and STAT2-deficient patients are unable to respond efficiently to stimulation by type I interferons and so our experiments provide insights into the importance of type I interferon signalling and the consequences of its impairment on human NK cell biology. Surprisingly, the NK cells of these patients display essentially normal phenotype and function.